Evidence map›Paper›PMID 37684015›Full record

ArticleThe Journal of international medical research2023

Genetic and clinical characteristics of ZNF408-related familial exudative vitreoretinopathy.

Xueying Tao, Liying He, Chao Cen, Ya Liu, Qi Li, Liyan Gong, Wenke Zhou, Chunmei Li

Open access · goldAbstract read
In one paragraph

Article in The Journal of international medical research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 33% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Xueying TaoDepartment of Ophthalmology and Otorhinolaryngology, Chongqing Health Center for Women and Children, Women and Children's Hospital of Chongqing Medical University, Chongqing, China.ORCID 0009-0000-4403-1886
Liying HeDepartment of Ophthalmology and Otorhinolaryngology, Chongqing Health Center for Women and Children, Women and Children's Hospital of Chongqing Medical University, Chongqing, China.
Chao CenDepartment of Ophthalmology and Otorhinolaryngology, Chongqing Health Center for Women and Children, Women and Children's Hospital of Chongqing Medical University, Chongqing, China.
Ya LiuDepartment of Ophthalmology and Otorhinolaryngology, Chongqing Health Center for Women and Children, Women and Children's Hospital of Chongqing Medical University, Chongqing, China.
Qi LiDepartment of Ophthalmology and Otorhinolaryngology, Chongqing Health Center for Women and Children, Women and Children's Hospital of Chongqing Medical University, Chongqing, China.
Liyan GongDepartment of Ophthalmology and Otorhinolaryngology, Chongqing Health Center for Women and Children, Women and Children's Hospital of Chongqing Medical University, Chongqing, China.
Wenke ZhouDepartment of Ophthalmology and Otorhinolaryngology, Chongqing Health Center for Women and Children, Women and Children's Hospital of Chongqing Medical University, Chongqing, China.
Chunmei LiDepartment of Ophthalmology and Otorhinolaryngology, Chongqing Health Center for Women and Children, Women and Children's Hospital of Chongqing Medical University, Chongqing, China.
Children's Hospital of Chongqing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo analyze the clinical and genetic characteristics of zinc finger protein 408 (

methodsNinety families from Chongqing and 16 families from Xinjiang were selected according to fundus lesion characteristics. Peripheral venous blood was collected from patients and their families; genomic DNA was extracted for whole exome sequencing. Relationships between genotype and phenotype in patients with

results

conclusionsThis study expands the spectrum of known

Indexed as

DNA-Binding ProteinsFamilial Exudative VitreoretinopathiesMutation, MissenseTranscription FactorsEast Asian PeopleGenotypeHumansPhenotypeDNA-Binding ProteinsTranscription FactorsZNF408 protein, humanclinical characteristicFamilial exudative vitreoretinopathygenotypemissense mutationphenotypewhole exome sequencingZNF408

Identifiers

PMID37684015
PMCPMC10492493
OpenAlexW4386532180

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.